719973009: Haim Munk syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...

\Keratoderma\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Hereditary diffuse palmoplantar keratoderma\Haim Munk syndrome

\Disorder of skin of lower limb\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Hereditary diffuse palmoplantar keratoderma\Haim Munk syndrome

\Disorder of skin of upper limb\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Hereditary diffuse palmoplantar keratoderma\Haim Munk syndrome

\Congenital anomaly of skin\Haim Munk syndrome

\Finding of head and neck region\Head finding\...

\Finding of head region\Finding of mouth region\Disorder of mouth\Congenital anomaly of mouth\Congenital abnormality of oral cavity\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Disorder of mouth\Disorder of teeth AND/OR supporting structures\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Disorder of mouth\Disorder of teeth AND/OR supporting structures\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Oral cavity finding\Congenital abnormality of oral cavity\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Oral cavity finding\Tooth finding\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Oral cavity finding\Tooth finding\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Oral cavity finding\Disorder of teeth AND/OR supporting structures\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Finding of head region\Finding of mouth region\Oral cavity finding\Disorder of teeth AND/OR supporting structures\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Disorder of jaw\Disorder of teeth AND/OR supporting structures\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Finding of head region\Disorder of jaw\Disorder of teeth AND/OR supporting structures\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Finding of head region\Disorder of jaw\Congenital anomaly of jaw\Congenital anomaly of tooth\Haim Munk syndrome

\Disorder of head\Disorder of mouth\Congenital anomaly of mouth\Congenital abnormality of oral cavity\Congenital anomaly of tooth\Haim Munk syndrome
\Disorder of head\Disorder of mouth\Disorder of teeth AND/OR supporting structures\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Disorder of head\Disorder of mouth\Disorder of teeth AND/OR supporting structures\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of mouth\Congenital abnormality of oral cavity\Congenital anomaly of tooth\Haim Munk syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of jaw\Congenital anomaly of tooth\Haim Munk syndrome
\Disorder of head\Disorder of jaw\Disorder of teeth AND/OR supporting structures\Tooth disorder\Hereditary disorder of tooth\Haim Munk syndrome
\Disorder of head\Disorder of jaw\Disorder of teeth AND/OR supporting structures\Tooth disorder\Disorder of tooth development\Malformation of tooth\Congenital anomaly of tooth\Haim Munk syndrome
\Disorder of head\Disorder of jaw\Congenital anomaly of jaw\Congenital anomaly of tooth\Haim Munk syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3318659013 Haim Munk syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3318660015 Haim Munk syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3318661016 Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Haim Munk syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Digestive system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Hereditary disorder of the integument	false	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Hereditary diffuse palmoplantar keratoderma	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Congenital anomaly of tooth	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	5
Haim Munk syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	6
Haim Munk syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	6
Haim Munk syndrome	Finding site	Tooth structure	false	Inferred relationship	Existential restriction modifier	6
Haim Munk syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Finding site	Tooth structure	true	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier	5
Haim Munk syndrome	Is a	Congenital anomaly of skin	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	3
Haim Munk syndrome	Interprets	Keratinization, function	false	Inferred relationship	Existential restriction modifier	3
Haim Munk syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Haim Munk syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Haim Munk syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Haim Munk syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Haim Munk syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Haim Munk syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	4
Haim Munk syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Haim Munk syndrome	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier	2
Haim Munk syndrome	Finding site	Skin structure of sole of foot	false	Inferred relationship	Existential restriction modifier	3
Haim Munk syndrome	Finding site	Skin structure of palmar area of hand	false	Inferred relationship	Existential restriction modifier	5
Haim Munk syndrome	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier	3
Haim Munk syndrome	Finding site	Entire skin of palmar area of hand	true	Inferred relationship	Existential restriction modifier	3
Haim Munk syndrome	Finding site	Entire skin of sole of foot	true	Inferred relationship	Existential restriction modifier	5
Haim Munk syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Haim Munk syndrome	Is a	Hereditary disorder of tooth	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3318659013	Haim Munk syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3318660015	Haim Munk syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3318661016	Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module